Clinical Research Coordinator Jobs in New Jersey
Clinical Research Coordinator jobs in New Jersey sit in one of the most active markets in the country, with strong demand across pharmaceutical development, academic medical research, and hospital-based clinical trials at every level from entry-level coordinators through senior and principal roles. Most hiring concentrates in Newark, New Brunswick, and Princeton, where employers such as Johnson & Johnson, Rutgers University Health, and Atlantic Health System have long-standing research operations. The most in-demand specialties are oncology trials, cardiovascular studies, and Phase II and III pharmaceutical research. Find a role that fits below and apply directly.
Find JobsOverview
Showing 5 of 13+ Clinical Research Coordinator jobs
Union, United States of America | Part time | Office-based | R1563895
Clinical Research Coordinator – Union, SC
Work Set-Up: On-site
Schedule Weekly Hours: 24 hours/week
About IQVIA
IQVIA is a global leader in advanced analytics, technology solutions, and clinical research services, dedicated to driving healthcare forward. We partner with the world’s leading pharmaceutical, biotechnology, and medical device companies to improve patient outcomes and accelerate innovation. Our team combines deep scientific expertise with cutting-edge technology to deliver high-quality data and insights that shape the future of clinical trials.
About the Role
We are seeking a Clinical Research Coordinator (CRC) to join our team and support clinical research studies under the supervision of a principal investigator. This role involves hands-on clinical procedures, community outreach, and ensuring the highest standards of care and compliance.
Key Responsibilities
Perform a variety of clinical procedures, including ECG, sample collection, and vital signs.
Coordinate clinical research studies and maintain compliance with protocols and Good Clinical Practice (GCP) guidelines.
Support study conducts by preparing study materials, setting up equipment, and planning logistical activities.
Recruit, screen, and orient patients, ensuring their safety and well-being throughout the study.
Collect and accurately record clinical data in case report forms (CRFs).
Collaborate with investigators and monitors, addressing queries and ensuring data quality.
Act as a patient advocate and maintain a safe environment in accordance with Health and Safety policies.
Qualifications
Bachelor’s degree preferred or equivalent combination of education and relevant experience.
Minimum 1+ years of relevant work experience in clinical research.
Working knowledge of clinical trials, GCP principles, and medical terminology.
Strong attention to detail and ability to establish effective working relationships.
Proficiency with EDC systems, data entry accuracy, and query management.
Please note: This position is not eligible for sponsorship.
#LI-CES #LI-DNP #LI-HCP #ONSITE
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com
IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe
IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
The potential base pay range for this role is $35.00-$42.00 per hour. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.Where you'll work
Office-based
You’ll work primarily from one of our office locations, collaborating closely with colleagues in a dynamic, team-oriented environment. This setting offers access to on-site resources, real-time interaction and opportunities to build strong relationships through in-person work.
Culture
Culture at IQVIA is built on a shared belief: that when people are empowered with better data, smarter technology and deeper expertise, they can change what’s possible for patients. Across every team and every corner of the globe, you’ll find colleagues who genuinely care — about the mission and about each other. That’s what makes this a place where people tend to stay, grow and do the best work of their careers.
Union, United States of America | Part time | Office-based | R1563895
Clinical Research Coordinator – Union, SC
Work Set-Up: On-site
Schedule Weekly Hours: 24 hours/week
About IQVIA
IQVIA is a global leader in advanced analytics, technology solutions, and clinical research services, dedicated to driving healthcare forward. We partner with the world’s leading pharmaceutical, biotechnology, and medical device companies to improve patient outcomes and accelerate innovation. Our team combines deep scientific expertise with cutting-edge technology to deliver high-quality data and insights that shape the future of clinical trials.
About the Role
We are seeking a Clinical Research Coordinator (CRC) to join our team and support clinical research studies under the supervision of a principal investigator. This role involves hands-on clinical procedures, community outreach, and ensuring the highest standards of care and compliance.
Key Responsibilities
Perform a variety of clinical procedures, including ECG, sample collection, and vital signs.
Coordinate clinical research studies and maintain compliance with protocols and Good Clinical Practice (GCP) guidelines.
Support study conducts by preparing study materials, setting up equipment, and planning logistical activities.
Recruit, screen, and orient patients, ensuring their safety and well-being throughout the study.
Collect and accurately record clinical data in case report forms (CRFs).
Collaborate with investigators and monitors, addressing queries and ensuring data quality.
Act as a patient advocate and maintain a safe environment in accordance with Health and Safety policies.
Qualifications
Bachelor’s degree preferred or equivalent combination of education and relevant experience.
Minimum 1+ years of relevant work experience in clinical research.
Working knowledge of clinical trials, GCP principles, and medical terminology.
Strong attention to detail and ability to establish effective working relationships.
Proficiency with EDC systems, data entry accuracy, and query management.
Please note: This position is not eligible for sponsorship.
#LI-CES #LI-DNP #LI-HCP #ONSITE
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com
IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe
IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
The potential base pay range for this role is $35.00-$42.00 per hour. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.Where you'll work
Office-based
You’ll work primarily from one of our office locations, collaborating closely with colleagues in a dynamic, team-oriented environment. This setting offers access to on-site resources, real-time interaction and opportunities to build strong relationships through in-person work.
Culture
Culture at IQVIA is built on a shared belief: that when people are empowered with better data, smarter technology and deeper expertise, they can change what’s possible for patients. Across every team and every corner of the globe, you’ll find colleagues who genuinely care — about the mission and about each other. That’s what makes this a place where people tend to stay, grow and do the best work of their careers.
See All 13 Clinical Research Coordinator Jobs in New Jersey
Find roles in New Jersey that match your experience and apply in just a few clicks.
Find JobsClinical Research Coordinator Jobs by City in New Jersey
Where New Jersey roles are concentrated, by current openings.
Clinical Research Coordinator Job Market in New Jersey
A snapshot from current New Jersey openings, updated as new roles post.
Who's Hiring
Top Industries Hiring
- Healthcare & Medical Services
- Medical Devices
- Consulting & Professional Services
What New Jersey Employers Look For
The qualifications that appear most often in clinical research coordinator jobs across New Jersey.
- Bachelor's degree in life sciences, nursing, or a related health field required
- ACRP or SOCRA clinical research certification preferred or required by most employers
- Minimum one to two years of experience managing clinical trial protocols and data
- Proficiency with electronic data capture systems such as REDCap or Medidata Rave
- Working knowledge of ICH-GCP guidelines and FDA regulatory requirements for clinical research
- Strong ability to coordinate with investigators, sponsors, and IRB for study compliance
Clinical Research Coordinator Jobs in New Jersey: Frequently Asked Questions
How do you become a clinical research coordinator in New Jersey?
Most clinical research coordinator positions in New Jersey require a bachelor's degree in a life science, nursing, or public health field. New Jersey does not issue a state-specific license for this role, but most employers expect candidates to hold or pursue certification through the Association of Clinical Research Professionals or the Society of Clinical Research Associates. Gaining experience through hospital research departments, academic medical centers like Rutgers, or pharmaceutical research sites in the Princeton corridor is the most common path.
How much do clinical research coordinators make in New Jersey?
Clinical research coordinators in New Jersey earn a median of about $207,030 a year, based on May 2025 Bureau of Labor Statistics wage data, ranging from around $136,840 for the lowest 10% to over $317,420 for the top 10%. Pay rises with experience, specialty, and employer.
Which companies hire clinical research coordinators in New Jersey?
Employers hiring clinical research coordinators in New Jersey right now include CenExel Clinical Research, Cooper University Healthcare, and SGS, based on current listings on Migrate Mate as of August 2026. New Jersey's dense concentration of pharmaceutical headquarters and academic medical centers means openings appear consistently throughout the year rather than in seasonal waves.
Which New Jersey cities have the most clinical research coordinator jobs?
Union, Camden, and Marlton have the most clinical research coordinator openings in New Jersey. The distribution reflects the state's pharmaceutical and biotech corridors, with New Brunswick anchored by Rutgers and major pharma campuses, Newark drawing from its large hospital network, and Princeton benefiting from the research operations of companies headquartered in the surrounding Mercer County area.
Are there remote clinical research coordinator jobs in New Jersey?
Yes, but they're rare. Most clinical research coordinator work requires on-site presence for patient interactions, specimen collection, and trial monitoring visits. About 0% of clinical research coordinator openings tied to New Jersey are remote or hybrid as of August 2026, and those tend to be in data management, regulatory affairs coordination, or sponsor-side monitoring roles rather than site-based coordinator positions.
How can I get hired as a clinical research coordinator in New Jersey with little or no experience?
The most realistic entry point is a research assistant or clinical trials assistant role at a New Jersey academic medical center such as Rutgers University Health or Hackensack Meridian Health, both of which hire into support roles that feed into coordinator positions. Candidates transitioning from adjacent roles like medical assistant, phlebotomist, or clinical data entry specialist have a strong conversion rate. Completing a GCP certification course before applying gives your application a concrete credential even without prior trial coordination experience.
Where can I find and apply to clinical research coordinator jobs in New Jersey?
You can find and apply to clinical research coordinator jobs in New Jersey on Migrate Mate, which lists current openings across the state. Find roles that match your experience and specialty, then apply directly to each one.
See All 13 Clinical Research Coordinator Jobs in New Jersey
Find roles in New Jersey that match your experience and apply in just a few clicks.
Find Jobs